[进行性家族性肝内胆汁淤积症的治疗进展]。

Q3 Medicine
T Liu, J S Wang
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引用次数: 0

摘要

进行性家族性肝内胆汁淤积症(PFIC)是导致儿童肝脏相关死亡或移植的重要原因。PFIC 的病谱在不断扩大,目前在线人类孟德尔遗传(OMIM)数据库已收录了 12 种 PFIC 类型。随着 PFIC 类型的增加以及某些类型在编号上的不一致,目前 PFIC 的编号分类较为混乱,因此该领域的专家建议除 PFIC 1-3 型外,使用相应的突变基因/蛋白质缺陷来命名不同类型的 PFIC。基因型与表型关系的明确和/或表型预测指标的建立,大大改善了对 PFIC 患者的管理。2021 年,欧盟和美国批准奥德韦希巴特和马拉利希巴特作为肠上皮细胞顶端钠离子依赖性胆汁酸转运体的抑制剂,用于治疗 PFIC 瘙痒症,扩大了 PFIC 的治疗选择范围。此外,针对特定突变的个性化治疗和新型基因疗法也很有前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Progress in the treatment of progressive familial intrahepatic cholestasis].

Progressive familial intrahepatic cholestasis (PFIC) is an important cause of liver-related death or transplantation in children. The PFIC spectrum is expanding, twelve types of PFIC are currently included in the Online Mendelian Inheritance in Man (OMIM) database. With the increase of PFIC types and the inconsistence of certain types in numbering, the current numbering classification of PFIC is confusing, so the experts in the field recommend using the corresponding mutant gene/ protein defect to name different type of PFIC except for PFIC type 1-3. The clarification of the genotype-phenotype relationship and/or the establishment of phenotypic predictors significantly improved the management of patients with PFIC. Odevixibat and maralixibat, inhibitors of the apical sodium ion-dependent bile acid transporter on the intestinal epithelial cells, were approved in European Union and the United States for the treatment of PFIC pruritus in 2021, expanding the treatment options for PFIC. Additionally, personalized treatments for specific mutations and novel gene therapy is promising.

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来源期刊
中华肝脏病杂志
中华肝脏病杂志 Medicine-Medicine (all)
CiteScore
1.20
自引率
0.00%
发文量
7574
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